Last Posted: Jul 22, 2018
- Consent and participation in the 100,000 Genomes Project – public attitudes
Genomics England, July 18, 2018 - Cancer Scientists Have Ignored African DNA in the Search for Cures
J Wapner, Newsweek, July 2018 - Ethical Issues of Using CRISPR Technologies for Research on Military Enhancement.
Greene Marsha et al. Journal of bioethical inquiry 2018 Jul - Incidental or secondary findings: an integrative and patient-inclusive approach to the current debate.
Saelaert Marlies et al. European journal of human genetics : EJHG 2018 Jul - Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background
KE Ormond et al, Genetics in Medicine, July 6, 2018 - [What if the sperm donor has a hereditary disease? Informed consent needed for sharing medical information].
van der Smagt J J et al. Nederlands tijdschrift voor geneeskunde 2017 161(0) D1445 - Genomic information and a person's right not to know: A closer look at variations in hypothetical informational preferences in a German sample.
Flatau Laura et al. PloS one 2018 13(6) e0198249 - How do consent forms for diagnostic high-throughput sequencing address unsolicited and secondary findings? A content analysis.
Vears D F et al. Clinical genetics 2018 Jun - Clinical evaluation of NIPS for women at advanced maternal age: a multicenter retrospective study.
Yu Bin et al. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2018 May 1-171 - Current ethical and legal issues in health-related direct-to-consumer genetic testing.
Niemiec Emilia et al. Personalized medicine 2017 Sep 14(5) 433-445
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